L. Lion‐François
发表
A. Szathmári,
C. Mottolese,
F. Di Rocco,
2020,
Child's Nervous System.
R. Delorme,
F. Rivier,
A. Afenjar,
2013,
Molecular genetics and metabolism.
N. Drouot,
P. Burbaud,
L. Cif,
2020,
Parkinsonism & related disorders.
J. Dumortier,
O. Guillaud,
A. Poujois,
2022,
Clinics and research in hepatology and gastroenterology.
V. des Portes,
D. Cheillan,
C. Jakobs,
2006,
Neurology.
J. Abdenur,
M. Tassini,
N. Dorison,
2018,
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.
A. Munnich,
C. Schwartz,
P. Pouwels,
2013,
Journal of Medical Genetics.
V. Herbillon,
A. Lachaux,
Rosa Yssaad-Fesselier,
2009,
Transplantation.
O. Guillaud,
V. Brun,
A. Lachaux,
2020,
Metallomics : integrated biometal science.
Ethan M. Goldberg,
J. Gécz,
M. Tress,
2022,
Genetics in Medicine.
V. de Lédinghen,
W. Meissner,
E. Broussolle,
2020,
Neurology.
J. Dumortier,
O. Guillaud,
A. Poujois,
2021,
Journal of pediatric gastroenterology and nutrition.
E. Favre,
A. Lachaux,
A. Brunet,
2017,
Journal of pediatric gastroenterology and nutrition.
S. Julia,
A. Afenjar,
O. Dulac,
2019,
Epilepsia.
F. Rivier,
S. Barbarot,
P. Meyer,
2016,
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.
D. Ville,
V. des Portes,
G. Lesca,
2014,
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.
S. Bendahhou,
D. Simkin,
B. Fontaine,
2011,
The Journal of physiology.
G. Michael,
V. Herbillon,
C. Mercier,
2020,
Journal of attention disorders.
S. Pinson,
F. Gueyffier,
V. des Portes,
2014,
Orphanet Journal of Rare Diseases.
M. Vidailhet,
A. Durr,
M. Polak,
2012,
Journal of Neurology, Neurosurgery & Psychiatry.
C. Mottolese,
D. Frappaz,
P. Thiesse,
2010,
Pediatric blood & cancer.
E. Broussolle,
S. Thobois,
J. Dumortier,
2016,
European Neurology.
G. Michael,
Sophie Garcia,
L. Guibaud,
2009,
Behavioral neuroscience.
F. Rivier,
S. Barbarot,
N. Dorison,
2018,
Child neuropsychology : a journal on normal and abnormal development in childhood and adolescence.
L. Christa,
C. Corne,
M. Milh,
2016,
JIMD Reports.
C. Sarret,
V. des Portes,
M. Massoud,
2020,
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.
R. Delorme,
F. Rivier,
A. Afenjar,
2012,
Orphanet Journal of Rare Diseases.
E. Christensen,
N. Dorison,
A. Lund,
2014,
Human mutation.
M. Till,
G. Lesca,
D. Sanlaville,
2019,
Molecular genetics & genomic medicine.
V. des Portes,
L. Guibaud,
C. Renard,
2008,
Archives de pédiatrie.
D. Ville,
A. Arzimanoglou,
G. Lesca,
2022,
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.
G. Michael,
V. Herbillon,
Sophie Garcia,
2014,
Neuropsychology.
F. Rivier,
S. Barbarot,
N. Dorison,
2017
.
E. Christensen,
N. Dorison,
A. Lund,
2014,
Human mutation.
L. Christa,
C. Corne,
M. Milh,
2016,
JIMD reports.
A. Arzimanoglou,
G. Lesca,
N. Chatron,
2018,
Epileptic disorders : international epilepsy journal with videotape.